OxyContin - 63629-3774-3 - (oxycodone hydrochloride)

Alphabetical Index


Drug Information of OxyContin

Product NDC: 63629-3774
Proprietary Name: OxyContin
Non Proprietary Name: oxycodone hydrochloride
Active Ingredient(s): 40    mg/1 & nbsp;   oxycodone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of OxyContin

Product NDC: 63629-3774
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022272
Marketing Category: NDA
Start Marketing Date: 20100808

Package Information of OxyContin

Package NDC: 63629-3774-3
Package Description: 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-3774-3)

NDC Information of OxyContin

NDC Code 63629-3774-3
Proprietary Name OxyContin
Package Description 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-3774-3)
Product NDC 63629-3774
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxycodone hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100808
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of OxyContin


General Information